Canonical Allele Identifier: CA1881271087
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130479716G= , CM000671.2:g.130479716G= GRCh38
NC_000009.11:g.133355103G= , CM000671.1:g.133355103G= GRCh37
NC_000009.10:g.132344924G= NCBI36
NG_011542.1:g.40010G=

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.689G= MANE Select NP_446464.1:p.Gly230=
ENST00000352480.10:c.689G= MANE Select ENSP00000253004.6:p.Gly230=
NM_000050.4:c.689G= NP_000041.2:p.Gly230=
NM_054012.3:c.689G= NP_446464.1:p.Gly230=
ENST00000352480.9:c.689G= ENSP00000253004.6:p.Gly230=
ENST00000372393.7:c.689G= ENSP00000361469.2:p.Gly230=
ENST00000372394.5:c.689G= ENSP00000361471.1:p.Gly230=
ENST00000467695.5:n.398G=
ENST00000470849.4:n.414G=
ENST00000492400.5:n.198G=
ENST00000493984.6:n.513-47G=
XM_005272200.2:c.689G= XP_005272257.1:p.Gly230=
XM_005272200.3:c.689G= XP_005272257.1:p.Gly230=
XM_011518705.1:c.803G= XP_011517007.1:p.Gly268=
XM_011518705.2:c.803G= XP_011517007.1:p.Gly268=
XM_017014729.1:c.785G= XP_016870218.1:p.Gly262=